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1  animals were undetectable in the absence of cocultivation.
2 ted with a decrease in embryo response after cocultivation.
3 gments, 56 were already regulated 24 h after cocultivation.
4 d Jurkat T reporter cell lines readily after cocultivation.
5 ed from infected cells to uninfected ones by cocultivation.
6 ven induced viremias detectable by leukocyte cocultivation.
7 hat were at least as high as transduction by cocultivation.
8 transduced on CH-296 as compared with BSA or cocultivation.
9 sed to transduce murine bone marrow cells by cocultivation.
10  in both A. nidulans and A. fumigatus during cocultivation.
11 different from that obtained after prolonged cocultivation (24 h, 96 h, and 21 days).
12 ned by varying the germination time prior to cocultivation and altering the bacterium: fungus ratio.
13  produce infectious virus, following explant cocultivation and that spontaneous reactivation could be
14 aponica, cv. Maybelle were explants used for cocultivation, and gene transfer was accomplished using
15            We now show, by using a sensitive cocultivation assay, that these RNA structures and their
16 ype ability to induce syncytia in an XC cell cocultivation assay.
17  vitro with wild-type kinetics in an explant cocultivation assay.
18                                              Cocultivation assays indicated that the difference in im
19  poor ability to recover infectious virus in cocultivation assays, even after CD8 depletion.
20 ced the amount of fusion observed in XC cell cocultivation assays, suggesting that this region influe
21                      Using long term stromal cocultivation assays, we studied the effects of FL on pr
22 n in vivo and in vitro assessed by BMDC OT-I cocultivation assays.
23 e outgrowth of HLA-matched lymphoma cells in cocultivation assays.
24 -dependent signaling during astrocyte-T cell cocultivation by a glutamate uptake inhibitor, l-asparti
25 v-target cell interface only after 30 min of cocultivation, concurrent with the first visible transfe
26 e to transmit the virus to uninfected MDM by cocultivation, confirming the infectiousness of this vir
27 s supernatant on FN 30/35 is as effective as cocultivation directly on producer cells; (2) recombinan
28                                     In vitro cocultivation experiments provided supporting evidence o
29                                           In cocultivation experiments, we demonstrate that although
30 hat hyperaccumulate glycogen were assayed by cocultivation experiments.
31 lyzed by plaque assay, PCR, and explantation cocultivation in both immunocompetent and cyclophosphami
32 es persistently upregulated during prolonged cocultivation included three genes (hfq, misR/phoP, and
33 cocci were also upregulated during prolonged cocultivation, indicating that our system models growth
34                                       EC-ASC cocultivation induced marked accumulation of activin A b
35                   Inclusion of L-cysteine in cocultivation medium lead to an improvement in transient
36                               A dual-species cocultivation model has been developed by using two ubiq
37  outgrew M2-del(29-31) virus in 4 days after cocultivation of a 100:1 ratio of M2-del(29-31) virus to
38                                              Cocultivation of ALL cell lines with packaging cell line
39                                        Here, cocultivation of an endophytic fungus Epicoccum dendrobi
40 expression from infections in vivo or during cocultivation of bacteria with tissue culture cells.
41                                              Cocultivation of cells individually expressing chimerae
42                                              Cocultivation of CTLs recognizing different CMV epitopes
43                                     However, cocultivation of EBV-infected B lymphocytes with uninfec
44 equencies of in vitro reactivation following cocultivation of explanted ganglia but reduced frequenci
45                                    In vitro, cocultivation of hepatocytes and nonparenchymal cells ha
46 ered by direct culture of their urine and by cocultivation of kidney tissue for up to 247 days after
47 que assay or reactivation ex vivo by explant cocultivation of latently infected murine trigeminal gan
48                                              Cocultivation of lymphocytes from HIV-1-infected persons
49                                              Cocultivation of lymphoid cell lines with reactivated iS
50 vated from latency following explanation and cocultivation of murine trigeminal ganglia with Vero cel
51                                     Finally, cocultivation of P. quadriseptata with Arabidopsis enhan
52 tralize primary HIV-1 strains in an assay of cocultivation of peripheral blood mononuclear cells (PBM
53                                              Cocultivation of primary hepatocytes with a plethora of
54 ation, we adopted and modified the method of cocultivation of single-captured bacterial cells in gel
55 tokine releasing assays were performed after cocultivation of T cells with irradiated Ramos SAg-expre
56 em cells (HSC) is currently only possible by cocultivation of target cells directly on producer cell
57 n the rates of virus reactivation by explant cocultivation of TG from latently infected WT or KO mice
58                                Nevertheless, cocultivation of TGN1412-treated T cells with HUVECs ind
59 of gusA transcripts within 18 to 24 hr after cocultivation of the bacteria with either tobacco or mai
60 When virus inhibition was examined after the cocultivation of transduced cells with chronically infec
61                                 When explant cocultivation of trigeminal ganglia was performed, the v
62 CD38- cells were stimulated with IL-3 during cocultivation on S17 stroma, on fibronectin, or in suspe
63 oviral vectors on CH-296-coated flasks or by cocultivation on vector-producing cells was studied in f
64                                      A 3-day cocultivation period follows, after which the cultures a
65 gamma nor TNF-alpha were required during the cocultivation period.
66 eneficial or antagonistic roles in microbial cocultivation systems, as is the case for antibiotic scr
67 vidually purified from such a mixed culture (cocultivation) through the use of a combination of a mul
68                                    Following cocultivation, viral antigens appeared first on PC12 cel
69  Superinfection by either cell-free HIV-1 or cocultivation was blocked.
70                           Virus isolation by cocultivation was positive for both CD4+ and CD8+ purifi
71 ould be recovered from the infected PBMCs by cocultivation with a canine indicator cell line, and we
72 heral blood mononuclear cells (PBMC) without cocultivation with a tissue culture cell line.
73 easing the inoculum strength of AM fungus or cocultivation with a wild-type nurse plant did not resul
74 an be successfully transformed using a short cocultivation with A. tumefaciens cells.
75 ncentration for selection is also used after cocultivation with Agrobacterium to mature the transform
76 y regulated (0.5% down-regulated) 48 h after cocultivation with Agrobacterium.
77                      An in vitro model of EC cocultivation with ASC was used, in which EC organized i
78 HLA-A2 HAM/TSP patient produced IFN-gamma by cocultivation with autologous CD4 cells, the main reserv
79 ns of primary rat hepatocytes are induced on cocultivation with Chinese hamster ovary cells engineere
80 was determined at intervals during prolonged cocultivation with confluent monolayers of the human res
81 test for PERV infection of human cells after cocultivation with either fetal porcine ventral mesencep
82 uman CD4(+) T cell lines were infected after cocultivation with epithelial cells at both early and la
83 ls and peripheral blood mononuclear cells by cocultivation with freeze-thawed Borrelia burgdorferi sp
84 ciens, and the resultant strain was used for cocultivation with germinated arthroconidia.
85 t infection with cell-free virus, as well as cocultivation with HHV-8-positive primary effusion lymph
86 med, the virus was recovered after 5 days of cocultivation with high efficiency.
87          The viral DNA was infectious, since cocultivation with human corneal fibroblasts (HCF) or hu
88 nd secretion of TNF-alpha was potentiated by cocultivation with IFN-gamma.
89 atant and NK cell supernatant generated from cocultivation with M. tuberculosis-infected monocytes al
90 of therapeutic outcome, while the results of cocultivation with macrophages were of moderate predicti
91 l methods using broth or agar, as well as by cocultivation with macrophages.
92 isolated from infected human cells following cocultivation with miniature swine peripheral blood mono
93 toencapsulation (e.g., double gel, Matrigel, cocultivation with nonparenchymal cells).
94 cted using this technique were transduced by cocultivation with retroviral producers expressing surfa
95  DMDS was depleted from the headspace during cocultivation with seedlings in bipartite Petri dishes,
96    HaCaT monolayers were slightly damaged by cocultivation with strain 35000-3 but this damage was mu
97     The appearance of infectious virus after cocultivation with SupT1 cells was delayed for the provi
98 ing capacity of astrocytes is increased upon cocultivation with T cells.
99 oductivity, and their restoring potency upon cocultivation with the Podocarpus gracilior microbiome.
100                                              Cocultivation with the virus producer line was consisten